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Treat-to-target study for improved outcome in polyarticular juvenile idiopathic arthritis
Ariane Klein1,2, Kirsten Minden3,4, Anton Hospach5
1Department of Pediatrics, Asklepios Kinderklinik Sankt Augustin, Sankt Augustin, Germany ariane.klein@web.de.
Insights
A treat-to-target (T2T) approach significantly improved remission rates in children with polyarticular juvenile idiopathic arthritis (pJIA) compared to routine care. This guided strategy is effective for managing pJIA, leading to better disease control.
Area of Science:
- Pediatric Rheumatology
- Clinical Immunology
- Inflammatory Diseases
Background:
- Juvenile idiopathic arthritis (JIA) is a common chronic inflammatory condition in children.
- Early, effective treatment is crucial to minimize long-term disease impact.
- Polyarticular JIA (pJIA) requires strategic management to achieve optimal outcomes.
Purpose of the Study:
- To evaluate if a guided treat-to-target (T2T) approach is superior to routine care for pJIA.
- To assess the efficacy of T2T in achieving clinical remission within 12 months.
- To compare treatment outcomes between T2T and unguided therapy in pJIA patients.
Main Methods:
- Patients with early, active pJIA were enrolled in a T2T protocol.
- Treatment targets included JADAS improvement, acceptable disease, minimal disease activity, and remission at specific intervals.
- Treatment modifications were made based on target achievement; T2T patients were compared to matched controls with unguided therapy.
Main Results:
- Significantly more T2T patients achieved JADAS remission (48% vs 32%) and JADAS-MDA (76% vs 59%) compared to controls.
- The T2T approach was feasible, with high rates of patients reaching treatment targets.
- T2T patients were more likely to receive biologics (50% vs 9% at 12 months).
Conclusions:
- The treat-to-target (T2T) strategy is feasible and more effective than unguided treatment for pJIA.
- High percentages of patients achieved minimal disease activity and remission using the T2T approach.
- Around half of the patients reached their therapy goals without requiring biologic agents.
Background:
Juvenile idiopathic arthritis is one of the most prevalent chronic inflammatory diseases in children. Evidence suggests that early effective treatment minimises the burden of disease during childhood and in further life. We hypothesise that a guided treat-to-target (T2T) approach is superior to routine care in polyarticular juvenile idiopathic arthritis (pJIA) in terms of reaching a clinical remission after 12 months of treatment.
Methods:
Patients with early and active pJIA were enrolled. Targets for treatment were the following: Recognisable Juvenile Arthritis Disease Activity Score (JADAS) improvement after 3 months, acceptable disease at 6 months, minimal disease activity at 9 months and as primary endpoint remission after 12 months. Initially, patients received methotrexate. Failure to meet a defined target required treatment modification at the specified intervals. The choice of biologics was not influenced by the protocol. Finally, T2T patients were compared with a cohort of matched controls of patients with pJIA with unguided therapy documented by BIKER.
Results:
Sixty-three patients were enrolled. Treatment targets after 3/6/9 and 12 months were reached by 73%/75%/77% and 48% of patients. Fifty-four patients completed the protocol. Compared with matched controls, on T2T guidance significantly more patients reached JADAS remission (48% vs 32%; OR 1.96 (1.1-3.7); p=0.033) and JADAS minimal disease activity (JADAS-MDA) (76% vs 59%; OR 2.2 (1.1-4.4); p=0.028). Patients from the T2T cohort received a biologic significantly more frequent (50% vs 9% after 12 months; OR 9.8 (4.6-20.8); p<0.0001).
Conclusion:
The T2T concept was feasible and superior to unguided treatment. High rates of patients reached JADAS-MDA and JADA remission after 12 months. Approximately half of the patients achieved their therapy goals without a biologic.
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